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American Journal of Human Genetics|September 19, 2024
Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesisEvon DeBose-Scarlett, Andrew K Ressler, Carol J Gallione, et al.American Journal of Human Genetics|November 14, 2007
DNA methylation signatures within the human brainChristine Ladd-Acosta, Jonathan Pevsner, Sarven Sabunciyan, et al.Epilepsia|January 24, 2007
Quantitative EEG asymmetry correlates with clinical severity in unilateral Sturge-Weber syndromeLaura A Hatfield, Nathan E Crone, Eric H Kossoff, et al.Journal of Molecular Neuroscience : MN|June 10, 2003
MANF: a new mesencephalic, astrocyte-derived neurotrophic factor with selectivity for dopaminergic neuronsPenka Petrova, Andrei Raibekas, Jonathan Pevsner, et al.Progress in Brain Research|January 1, 2004
Discovering novel phenotype-selective neurotrophic factors to treat neurodegenerative diseasesPenka S Petrova, Andrei Raibekas, Jonathan Pevsner, et al.American Journal of Human Genetics|October 2, 2002
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)Evan Reid, Mark Kloos, Allison Ashley-Koch, et al.Stroke|August 28, 2004
Polymorphisms in genes involved in inflammatory and angiogenic pathways and the risk of hemorrhagic presentation of brain arteriovenous malformationsLudmila Pawlikowska, Mary N Tran, Achal S Achrol, et al.Proceedings of the National Academy of Sciences of the United States of America|May 25, 2004
Gene expression alterations over large chromosomal regions in cancers include multiple genes unrelated to malignant progressionBrett G Masayesva, Patrick Ha, Elizabeth Garrett-Mayer, et al.Plos Genetics|December 14, 2012
Dissection of a quantitative trait locus for PR interval duration identifies Tnni3k as a novel modulator of cardiac conductionElisabeth M Lodder, Brendon P Scicluna, Annalisa Milano, et al.Pediatric Neurology|July 15, 2020
Suicide Screening in Sturge-Weber Syndrome: An Important Issue in Need of Further StudyAlison J Sebold, Amelia S Ahmed, Taylor C Ryan, et al.Pageof 27